Free A, Dorman C J
Department of Microbiology, Moyne Institute of Preventive Medicine, University of Dublin, Trinity College, Ireland.
Mol Microbiol. 1995 Oct;18(1):101-13. doi: 10.1111/j.1365-2958.1995.mmi_18010101.x.
The H-NS protein of enteric bacteria is one of the major proteins of the bacterial nucleoid and seems to play an important role in nucleoid structure. Transcription of the hns gene encoding the H-NS protein appears to be negatively regulated by H-NS itself both in vitro and in vivo. We have examined the role of this mode of regulation in wild-type cells in vivo. We find that hns transcription is down-regulated when DNA synthesis is blocked in growing cells, in a manner that is dependent upon continuing H-NS protein synthesis. These data suggest that hns autoregulation serves to match de novo H-NS synthesis to the demands of DNA synthesis and may maintain a relatively constant H-NS:DNA ratio. It has previously been suggested that hns transcription is activated as cells enter stationary phase, which would require a complete relaxation of autoregulatory control given that DNA synthesis decreases at this time. However, we show here that levels of hns mRNA in fact decline at the onset of stationary phase in a manner fully consistent with the autoregulation model. We also fail to detect any significant accumulation of the H-NS protein in stationary phase.
肠道细菌的H-NS蛋白是细菌类核的主要蛋白之一,似乎在类核结构中发挥重要作用。编码H-NS蛋白的hns基因的转录在体外和体内似乎都受到H-NS自身的负调控。我们已经研究了这种调控模式在野生型细胞体内的作用。我们发现,当生长中的细胞DNA合成受阻时,hns转录会下调,其方式依赖于持续的H-NS蛋白合成。这些数据表明,hns自调控有助于使新生H-NS合成与DNA合成需求相匹配,并可能维持相对恒定的H-NS:DNA比率。此前有人提出,当细胞进入稳定期时hns转录被激活,鉴于此时DNA合成减少,这将需要完全放松自调控控制。然而,我们在此表明,hns mRNA水平实际上在稳定期开始时下降,其方式与自调控模型完全一致。我们也未能检测到稳定期H-NS蛋白有任何显著积累。